Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by a range of physical, mental, and behavioral problems including chronic hunger, poor muscle tone, and developmental delays. To accurately diagnose this condition, the Prader-Willi Syndrome FISH (Fluorescence In Situ Hybridization) test is employed, which is a sophisticated genetic test designed to detect abnormalities specific to the chromosome 15 region associated with PWS.
The FISH test involves using fluorescent probes that bind to specific parts of chromosomes, making it possible to visualize genetic abnormalities under a microscope. This method is highly effective in identifying the deletion or uniparental disomy (UPD) of chromosome 15, which are common genetic markers of Prader-Willi Syndrome.
In the United Arab Emirates, DNA Labs UAE is a reputable facility that offers the Prader-Willi Syndrome FISH Test. The test is priced at 1050 AED, providing a crucial diagnostic tool for families and physicians dealing with the potential diagnosis of PWS. The results from this test can help in planning appropriate management and therapeutic strategies for individuals diagnosed with Prader-Willi Syndrome, ultimately improving their quality of life.
Replication Factor C1 Mutation Screening (RFC1 - 80G>A Test) is a specialized genetic test offered by DNA Labs UAE, designed to identify mutations in the RFC1 gene, specifically the 80G>A mutation. This mutation can have significant implications for cellular DNA replication and repair mechanisms, potentially leading to various genetic disorders or influencing the risk of developing certain diseases. The test involves analyzing the individual's DNA to detect the presence of the 80G>A mutation in the RFC1 gene, providing valuable insights into genetic health and predispositions. Priced at 1050 AED, this test is a crucial tool for individuals seeking a deeper understanding of their genetic makeup, particularly those with a family history of genetic disorders linked to the RFC1 gene. By identifying this mutation, healthcare providers can offer personalized medical advice, preventive measures, or targeted treatments to manage or mitigate associated health risks.
The "15-20 Slide and Block Test" offered by DNA Labs UAE is a comprehensive diagnostic assessment designed to analyze a specific range of biological samples. This test, priced at 1050 AED, is meticulously carried out in the state-of-the-art facilities of DNA Labs UAE, a reputable institution known for its advanced diagnostic and research capabilities. The test involves the detailed examination of 15 to 20 slides or blocks, which could encompass a variety of sample types depending on the diagnostic requirement. This could include tissues, cells, or other biological materials that need in-depth analysis for medical, research, or forensic purposes.
DNA Labs UAE employs cutting-edge technology and follows stringent protocols to ensure the accuracy and reliability of the test results. The process involves preparing the slides or blocks, followed by a detailed microscopic examination and analysis by highly qualified and experienced professionals. This test is crucial for diagnosing diseases, understanding pathological conditions, or for academic and research purposes, providing invaluable insights into the sample's microscopic structure and function.
Given its comprehensive nature and the expertise involved, the test cost of 1050 AED is justified, offering clients access to world-class diagnostic services. DNA Labs UAE also ensures confidentiality and timely delivery of test results, making it a preferred choice for individuals and professionals seeking detailed and reliable analysis.
Sickle Cell Disease Mutation Screening Test is a crucial diagnostic tool offered at DNA Labs UAE, aimed at identifying the presence of mutations in the HBB gene, which are responsible for sickle cell disease (SCD). This genetic condition affects the shape and functionality of red blood cells, leading to various health complications such as pain, infections, and anemia. The test, priced at 1050 AED, involves analyzing a sample of the patient's DNA to detect specific mutations linked to SCD. This screening is particularly beneficial for individuals with a family history of the disease or those belonging to regions where the condition is prevalent. By providing early detection, the Sickle Cell Disease Mutation Screening Test enables timely interventions and informed decisions about managing the condition, thereby improving the quality of life for those affected.
The "Small Biopsy Bottle No 10 Test" is a specific diagnostic procedure available at DNA Labs UAE, designed to analyze small biopsy samples for a variety of medical purposes. This test involves collecting a small tissue sample from the patient, which is then securely placed in a designated biopsy bottle, labeled as No 10, for precise handling and analysis. The procedure is critical for diagnosing diseases, understanding the extent of tissue abnormality, and guiding treatment plans.
DNA Labs UAE, a reputable laboratory known for its advanced diagnostic services, offers this test for a cost of 1050 AED. The laboratory utilizes state-of-the-art technology and employs highly skilled professionals to ensure accurate and reliable results. Patients opting for the Small Biopsy Bottle No 10 Test at DNA Labs UAE can expect a thorough examination of their biopsy sample, contributing to effective disease management and treatment decisions.
The "TELAML ALL Test" is a specialized diagnostic procedure designed to identify the TEL-AML1 gene fusion, which is commonly associated with acute lymphoblastic leukemia (ALL). This genetic anomaly is crucial for the diagnosis, prognosis, and management of ALL, a type of cancer that affects the white blood cells and can progress rapidly if left untreated. The test involves analyzing the patient's DNA to detect the presence of the TEL-AML1 fusion gene, which can influence treatment decisions and help predict the patient's response to therapy.
Performed at DNA Labs UAE, a reputable facility known for its advanced diagnostic technologies and expert staff, the test ensures accuracy and reliability. The cost of the TELAML ALL Test is set at 1050 AED, making it a valuable investment for individuals seeking comprehensive insights into their health status concerning acute lymphoblastic leukemia. By opting for this test at DNA Labs UAE, patients and healthcare providers can access crucial genetic information that plays a significant role in tailoring treatment strategies for optimal outcomes.
The "Trisomy 12 CLL Test" is a specialized diagnostic procedure designed to detect the presence of an extra chromosome 12 in the genetic material of individuals suspected of having Chronic Lymphocytic Leukemia (CLL). This genetic anomaly, known as Trisomy 12, is a common chromosomal abnormality associated with CLL, a type of cancer that affects the white blood cells and can impact the body's ability to fight infections.
Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves the collection of a blood sample from the patient. The sample is then analyzed using sophisticated genetic sequencing techniques to identify the presence of Trisomy 12, which can provide valuable information regarding prognosis and may influence treatment decisions.
The cost of the Trisomy 12 CLL Test at DNA Labs UAE is set at 1050 AED. This investment in health can be crucial for individuals with CLL or those at risk, as it enables timely and informed decisions regarding their medical care. By identifying Trisomy 12, healthcare providers can tailor treatment plans more effectively, potentially improving patient outcomes.
The "Trisomy 8 AML Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect the presence of an extra chromosome 8 in the cells of individuals suspected of having Acute Myeloid Leukemia (AML). This condition, known as Trisomy 8, is a chromosomal abnormality that can contribute to the development and progression of AML, a type of cancer that affects the blood and bone marrow. The test plays a crucial role in the diagnosis, prognosis, and management of AML by providing essential genetic information that can guide treatment decisions. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test is priced at 1050 AED, ensuring accessibility to crucial diagnostic services for those in need.
The William's Syndrome FISH (Fluorescent In Situ Hybridization) Test is a specialized diagnostic procedure used to detect the presence of William's Syndrome, a genetic disorder characterized by developmental delays, cardiovascular disease, distinctive facial features, and a unique personality profile. This test specifically looks for deletions in the region of chromosome 7 that includes the elastin gene, which is typically missing in individuals with William's Syndrome. By using fluorescent probes that bind to specific parts of the chromosome, this method allows for a clear visualization of the genetic material under a microscope, making it possible to identify the absence of the critical region.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers families and physicians crucial information for the management and treatment of the condition. The cost of the William's Syndrome FISH Test at DNA Labs UAE is set at 1050 AED. This investment covers the sophisticated technology and expert analysis required to accurately diagnose this genetic disorder, providing essential insights for medical care and support planning for affected individuals and their families.
The "X and Y Sex Mismatch Bone Marrow Transplant Test" is a sophisticated diagnostic procedure offered by DNA Labs UAE, aimed at ensuring the compatibility and success of bone marrow transplants. This test is particularly crucial in cases where the donor and recipient are of opposite sexes, as it meticulously analyzes the sex chromosomes (X and Y) to identify any potential mismatches that could affect the transplant's outcome. By examining the genetic compatibility between the donor's and recipient's sex chromosomes, this test plays a vital role in minimizing the risk of graft-versus-host disease (GVHD) and other complications associated with bone marrow transplantation. Priced at 1050 AED, this test represents a critical investment in the success and safety of bone marrow transplant procedures, providing both patients and medical professionals with essential information for making informed decisions about transplantation strategies.
